THOR Red Light Therapy Bed Recall: Gas Strut Detachment Risk

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Recalling firmThor Photomedicine LtdWatermeadow House · Chesham, N/A

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✎ GovInfoNow plain-language explainer

What happened, in plain English

THOR Photomedicine Ltd is recalling specific red light therapy beds due to a risk that the canopy could detach from the bed. This could make it difficult to lift the canopy safely during use.

Why it’s dangerous

The bed's ball stud components can fail, causing the gas strut on one side to detach from the canopy. This makes it difficult to lift the canopy safely during use, potentially leading to injury if the canopy falls.

Who’s affected

Owners of the recalled THOR G041 POD whole body red light therapy beds with serial numbers 3001, 3002, 3003, 3004, 3006, 3008, or 3009 are affected. Users who lift the canopy without proper support are most at risk.

How to tell if you have this one

Check your THOR G041 POD whole body red light therapy bed's serial number. The recalled units have serial numbers 3001, 3002, 3003, 3004, 3006, 3008, or 3009.

Brand
THOR
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Serial Number
Identify your THOR G041 POD bed's serial number to confirm if it's in the recall list.
Stop Using Bed
If your bed has a recalled serial number, stop using it immediately until you receive further instructions.

✎ GovInfoNow

Questions people ask

Why is this bed being recalled?

The bed's ball stud components can fail, causing the gas strut on one side to detach from the canopy, making it difficult to lift safely.

What should I do if I have a recalled bed?

Check your serial number against the list (3001, 3002, 3003, 3004, 3006, 3008, 3009). If it's recalled, stop using it immediately.

Is there a fix for this issue?

The recall record does not mention a fix or remedy.

Take action

Contact THOR

We’ve drafted a message you can send THOR to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0454-2024 — THOR THOR

Hello,

I own a THOR that is covered by recall Z-0454-2024 from THOR.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-0454-2024 (September 13, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0454-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Thor Photomedicine Ltd recalls G041 POD, THOR NOVO GEN 2.0 XL whole body red light therapy bed, model S1177

Use caution until it’s fixed